...
首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >SYNTHESIS OF 3-OXOAZACYCLOHEPT-4-ENES BY RING-CLOSING METATHESIS.APPLICATION TO THE SYNTHESIS OF AN INHIBITOR OF CATHEPSIN K
【24h】

SYNTHESIS OF 3-OXOAZACYCLOHEPT-4-ENES BY RING-CLOSING METATHESIS.APPLICATION TO THE SYNTHESIS OF AN INHIBITOR OF CATHEPSIN K

机译:闭环置换合成3-OXOAZACYCLOHEPT-4-ENE ..在合成组织蛋白酶K抑制剂中的应用

获取原文
获取原文并翻译 | 示例

摘要

The ring-closing metathesis allows the formation of 3-oxoazacyclohept-4-enes from but-3-enamine.By using this methodology,the synthesis of an inhibitor of cathepsin K was achieved in 10 steps from but-3-enamine.Seven-membered ring amino compounds are present in a great variety of natural and non-natural products which possess interesting biological properties.These molecules have stimulated the development of an array of methods for their synthesis.
机译:闭环复分解允许由丁3-烯胺形成3-氧杂氮杂环庚4-烯。通过这种方法,从丁3-烯胺分十步合成了组织蛋白酶K抑制剂。元环有机化合物存在于多种天然和非天然产物中,这些产物具有令人感兴趣的生物学特性。这些分子刺激了其合成方法的发展。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号